Nearly 10% of postmarket device safety reports in MAUDE were submitted over 6 months after the safety event occurred.

Over 1.2 million medical device adverse event reports were not submitted to the US Food and Drug Administration (FDA) within the deadline set by federal regulations, finds an analysis of recent data ...

Last month, a non-peer-reviewed study commissioned by Moms Across America alleged that Girl Scout Cookies had toxins in them.

It’s time to revamp the FDA’s “generally recognized as safe,” or GRAS, program that allows companies to add untested ...

We've all seen the various inspection labels at the grocery store and heard news about food recalls. But what's the actual ...

The U.S. Food and Drug Administration said on Monday it will not take action against compounding pharmacies making copies of ...

Time is running out on meeting rules from both food safety agencies; here’s what you need to be working on this year.

New SEC filings from pharmaceutical companies reveal Donald Trump and Elon Musk’s cost-cutting measures could slow drug ...

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The province announced Tuesday it will be making changes to legislation and regulations to crack down on drug trafficking and on people using fentanyl and methamphetamine. Police will be given ...

This is similar to the defence in section 5(2) RTA 1988. The relevant drugs are listed in the Drug Driving (Specified Limits) (England and Wales) Regulations 2014 and the Drug Driving (Specified ...

Spotify CEO pushes EU to crack down on Apple, accusing the tech giant of exploiting its influence to bypass Big Tech rules Daniel Ek escalates Spotify’s battle against Apple, urges regulators to ...